@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP727970.RAlVBZGtczP0OdFSib7MS7zNhZ9mDbvfUIRc5SWtBdw2Y
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP727970.RAlVBZGtczP0OdFSib7MS7zNhZ9mDbvfUIRc5SWtBdw2Y130_head
{
this:
np:hasAssertion
dgn-np:NP727970.RAlVBZGtczP0OdFSib7MS7zNhZ9mDbvfUIRc5SWtBdw2Y130_assertion
;
np:hasProvenance
dgn-np:NP727970.RAlVBZGtczP0OdFSib7MS7zNhZ9mDbvfUIRc5SWtBdw2Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP727970.RAlVBZGtczP0OdFSib7MS7zNhZ9mDbvfUIRc5SWtBdw2Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP727970.RAlVBZGtczP0OdFSib7MS7zNhZ9mDbvfUIRc5SWtBdw2Y130_assertion
a
np:Assertion
.
dgn-np:NP727970.RAlVBZGtczP0OdFSib7MS7zNhZ9mDbvfUIRc5SWtBdw2Y130_provenance
a
np:Provenance
.
dgn-np:NP727970.RAlVBZGtczP0OdFSib7MS7zNhZ9mDbvfUIRc5SWtBdw2Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP727970.RAlVBZGtczP0OdFSib7MS7zNhZ9mDbvfUIRc5SWtBdw2Y130_assertion
{
miriam-gene:7415
a
ncit:C16612
.
lld:C1368019
a
ncit:C7057
.
dgn-gda:DGN25b00b47c8700c581bc24cd22539e581
sio:SIO_000628
miriam-gene:7415
,
lld:C1368019
;
a
sio:SIO_001121
.
}
dgn-np:NP727970.RAlVBZGtczP0OdFSib7MS7zNhZ9mDbvfUIRc5SWtBdw2Y130_provenance
{
dgn-np:NP727970.RAlVBZGtczP0OdFSib7MS7zNhZ9mDbvfUIRc5SWtBdw2Y130_assertion
dcterms:description
"[New insights from the biology of adolescent osteosarcomas, VCP and SQSTM1 mutations now defined in patients with Paget's disease, and emerging evidence that stromal lesions are present in patients with Paget's disease are changing the way we think about the pathogenesis of PDB and the rare complication of pagetic osteosarcomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:17229010
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP727970.RAlVBZGtczP0OdFSib7MS7zNhZ9mDbvfUIRc5SWtBdw2Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:22+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}